Canonical Allele Identifier: PA916014783
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408208
ClinVar RCV Id: RCV000468822 RCV002496761 RCV003477955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asp229Asn
CA8252858
NM_001286167.3:c.685G>A